Hypokalaemic periodic paralysis due to a novel ATP1A2 mutation: a new periodic paralysis gene?

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Bibliographic Details
Published in:Neuromuscular disorders : NMD 2017-03, Vol.27, p.S33-S33
Main Authors: Matthews, E, Zanoteli, E, Scalco, R.S, O’Callaghan, B, Sud, R, McCall, S, Hanna, M.G, Sampedro Castenada, M, Männikkö, R, Poulson, H
Format: Article
Language:English
Subjects:
Neurology
Online Access:Get full text
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ISSN:0960-8966
DOI:10.1016/S0960-8966(17)30317-6